Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18889Generated: October 25, 2026

2-Amino-5-chlorobenzophenone → N-(2-Benzoyl-4-chloro-phenyl)-4-methanesulfonyl-benzenesulfonamide

https://huagongshe.com/reaction/18889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-chlorobenzophenoneHCID 12870—
Reactant4-Methanesulfonylbenzene-1-sulfonyl chlorideHCID 2735182—
ProductN-(2-Benzoyl-4-chloro-phenyl)-4-methanesulfonyl-benzenesulfonamideHCID 11408313—

Reaction Steps

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 115 mg of (2-amino-5-chloro-phenyl)-phenyl-methanone and 127 mg of 4-Methanesulfonyl-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 2.92 (s, 3H), 7.34 (m, 3H), 7.434 (m, 2H), 7.51 (dd, 1H, J=8.8 Hz, 2.4 Hz), 7.60 (m, 1H), 7.75 (d, 1H, J=8.8 Hz), 7.80-7.86 (m, 4H), 9.86 (b, 1H). MS: m/z 450.9 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741519B2
Source datasetuspto-grants-2010_06
ORD IDord-4fd6963b18fb454382e486e6af2332c3
Source noteuspto-grants-2010_06